SOP.9. Manually counting and spiking of cells in blood

Transcription

1 Circulating Tumor Cells TheRapeutic APheresis: a novel biotechnology enabling personalized therapy for all cancer patients SOP.9. Manually counting and spiking of cells in blood

2 Introduction This Standard Operating Procedure (SOP) describes the spiking of cell manually in blood samples. These samples will be used to determine the recovery of cell line CTC after CellSearch, CellSearch Waste Filtration (SOP.3.) and staining (SOP.6.). This is SOP.9. Manually counting and spiking; version /VS Workflow of procedures in the CTCTrap program Validation Study SOP.9. Manually counting and spiking; v of 8 University of Twente

3 SOP.9. Manually counting and spiking of cells in blood For the validation study, cells will be manually spiked in healthy donor (HD) blood samples. The cell lines used for this are PC3 prostate cancer cells and MDA-MB-231 breast cancer cells. Both of these cells are (partially) EpCAM negative and will be found after CellSearch and after filtration. Introduction Cells Preparation Cells Microscope slide CellSave blood sample Counting Spiking Counts... 7 Tubes collection Tubes collection Tubes collection Shipping Addresses... Error! Bookmark not defined. SOP.9. Manually counting and spiking; v of 8 University of Twente

4 1. Cells Time: 30 min Note: Cells have to be added to the CellSave blood sample on the day of draw. 1. Dissociate the cells for spiking with trypsin/edta. After dissociation, transfer the cells to a tube and add CellSave. Add 100 µl CellSave for every 5 ml medium with cells. Mix thoroughly (see Figure 1). 2. Determine the concentration of cells with a counting chamber. 2. Preparation Time: 30 min 2.1. Cells 3. Dilute the cells you will spike to a concentration of 15,000 cells per ml in 1 or 0.5 ml PBS/BSA1%. This will be 15 cells per µl. 4. Add Hoechst at 2µg/mL final concentration and incubate for 10 minutes at 37 C (see Figure 2) Microscope slide 5. Put the glass microscope slides in PBS/BSA1% for 10 minutes (see Figure 3). 6. Rinse the slide with MQ and blow dry with air CellSave blood sample 7. Mix the CellSave blood sample thoroughly. Divide the blood samples over the conical tubes with each 7.5 ml blood. 8. Label each tube with a code, separating for each site: unspiked healthy donor blood (HD) (A), spiked PC3 cells (B), spiked MDA-MB-231 cells (C). 3. Counting Time: 20 min per slide for counting and spiking 9. Add 10 drops of 2 µl cell suspension on the edge of the slide (see Figure 4). This will yield approximately 10x 30 cells and can be counted before all the drops dry out. 10. Count the cells with aid of a cell counter under the microscope with 4x magnification using a UV filter cube. 11. Note the amount of cells in each drop (in case you go wrong during counting). SOP.9. Manually counting and spiking; v of 8 University of Twente

5 Figure 1 Medium with cells after dissociation, with manually added CellSave (from stock or from CellSave tubes). Figure 3 Incubating microscope slides in PBS/BSA1%. Figure 2 Dilution of cells to cells/ml for counting with Hoechst for nuclei staining. Figure 4 Ten droplets of 2 µl with cells on a microscope slide for easy manual counting. Figure 5a In the droplet you can count 34 Hoechst positive cells. Small specks can be easily distinguished from the cells. This image was taken with a 4x objective. Figure 5b After spiking the cells from the glass slide, the imprint of the drops can be easily spotted with the microscope and any remaining cells in it, as well. Here 1 cell remained behind, so this is deducted from the total count. 4. Spiking 12. Use 1 ml CellSearch Dilution buffer (stored at RT) to rinse the slide and flow the cells in the blood sample (see Figure 5). SOP.9. Manually counting and spiking; v of 8 University of Twente

6 Be careful not to spill, because then you will lose cells. 13. Check the clean slide under the microscope and count the remaining cells. 14. Fill in the tables below, by adding all the counts from every drop, and then deducting the amount of cells that remained on the slide. 15. Add 1 ml of CellSearch Dilution buffer to the HD blood tube as well. Figure 6 Spiking the cells in the blood with 1 ml CellSearch Dilution Buffer. Figure 7 Spiked blood samples designated with cell type and site. Tube A is wrapped for shipment. SOP.9. Manually counting and spiking; v of 8 University of Twente

7 5. Counts Tubes collection 1 Operator Date: - - Site Cell count per cell type HD (A) PC3 (B) MDA-MB-231 (C) ICR IGR IOV LMU UFT UT Tubes collection 2 Operator Date: - - Site Cell count per cell type HD (A) PC3 (B) MDA-MB-231 (C) ICR IGR IOV LMU UFT UT SOP.9. Manually counting and spiking; v of 8 University of Twente

8 Tubes collection 3 Operator Date: - - Site Cell count per cell type HD (A) PC3 (B) MDA-MB-231 (C) ICR IGR IOV LMU UFT UT 6. Shipping 16. Collect the tubes for shipment. Make sure the tubes are securely closed with a conical tube cap. Wrap parafilm around the the caps (see Figure 6). 17. Isolate the tubes sufficiently to protect them from temperature changes during shipment. Note: All tubes have to be shipped on the day of blood draw, to ensure processing the sample 24 hours after draw. SOP.9. Manually counting and spiking; v of 8 University of Twente